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Peri-implantitis, Comparing Treatments 970 nm Laser and Mucosal Flap Surgery

Peri-Implantitis Clinical Trial

Official title:
Comparing Treatment of Peri-implantitis With Either 970 nm Laser or Conventional Mucosal Flap Surgery - a Prospective Randomized Controlled Trial

Clinical Trial Summary

A clinical trial comparing laser treatment and conventional mucosal flap surgery for treatment of peri-implantitis. The main aim of the study is to evaluate if treatment of peri-implantitis with 970 nm laser combined with scaling and root planning (SRP) is clinically comparable to conventional mucosal flap surgery in terms of pocket probing depth reduction.

Clinical Trial Description

The present project aims to evaluate a novel method in treating peri-implantitis, with focus on decreasing the patient's suffering as well as disease progression. Peri-implantitis has a direct influence on both physical and psychological wellbeing and have been related to difficulty in chewing due to loss of implants, bad esthetic appearance as well as high costs. Therefore, it is of importance for the individual as well as for the society to thoroughly investigate any new treatment approaches. The study is a prospective randomized clinical trial comparing laser treatment (test group) and conventional mucosal flap surgery (active control group). Assessment of clinical variables at baseline and after 6 months. Patient reported outcomes at baseline, directly after treatment and after 10 days. Primary Objective: To evaluate if treatment of peri-implantitis with 970 nm laser combined with scaling and root planning (SRP) is clinically comparable to conventional mucosal flap surgery in terms of pocket probing depth reduction. Secondary Objectives: - To evaluate other clinical and radiological variables connected to peri-implantitis and the inflammation surrounding the dental implant. - To evaluate the patient experience of treatment of peri-implantitis. - To evaluate the inflammatory and microbial response after laser treatment ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04249024
Study type Interventional
Source Karolinska Institutet
Contact
Status Completed
Phase N/A
Start date September 25, 2019
Completion date June 21, 2022
View Details
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